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Genetic Polymorphisms of IL-17F and TRAF3IP2 Could Be Predictive Factors of the Long-Term Effect of Infliximab against Crohn’s Disease


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Title: Genetic Polymorphisms of IL-17F and TRAF3IP2 Could Be Predictive Factors of the Long-Term Effect of Infliximab against Crohn’s Disease
Authors: Urabe, Shigetoshi / Isomoto, Hajime / Ishida, Tetsuya / Maeda, Kazumi / Inamine, Tatsuo / Kondo, Shinji / Higuchi, Norihide / Sato, Kayoko / Uehara, Ryohei / Yajima, Hiroyuki / Machida, Haruhisa / Chen, Chun Chuan / Fukuda, Yasuhiro / Takeshima, Fuminao / Nakao, Kazuhiko / Tsukamoto, Kazuhiro
Issue Date: 2015
Publisher: Hindawi Publishing Corporation
Citation: BioMed Research International, 2015, 416838; 2015
Abstract: Background. We aimed to identify certain genes related to response to infliximab (IFX) and biomarkers to predict the IFX effect for Japanese Crohn's disease (CD) patients by performing an association study of single nucleotide polymorphisms (SNPs) in candidate genes in the interleukin-(IL-) 17 signaling pathway with response to IFX after 1 year of treatment. Methods. A total of 103 patients were divided into two groups, responders and nonresponders. Twenty-eight tag SNPs in 5 genes were genotyped. The frequencies of alleles and genotypes of each SNP were compared between responders and nonresponders in three different inheritance models. A genetic test was performed using a combination of the associated SNPs as biomarkers. Results. Multivariate logistic regression analysis indicated that the four variable factors, concomitant use of immunomodulators, penetrating disease, a G/G genotype of rs766748 in IL-17F, and a C/C or C/A genotype of rs1883136 in TRAF3IP2, independently contributed to response to IFX after 1 year of treatment. Genetic test using the polymorphisms of these genes perfectly predicted the responder and nonresponder CD patients with both concomitant use of immunomodulators and penetrating disease. Conclusion. IL17F and TRAF3IP2 are one of IFX-related genes, useful as biomarkers of IFX response, and may be target molecules for new therapeutic drugs.
URI: http://hdl.handle.net/10069/36098
ISSN: 23146133
DOI: 10.1155/2015/416838
Rights: © 2015 Shigetoshi Urabe et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Type: Journal Article
Text Version: publisher
Appears in Collections:Articles in academic journal

Citable URI : http://hdl.handle.net/10069/36098

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